Structure of PDB 1s3e Chain A Binding Site BS01
Receptor Information
>1s3e Chain A (length=499) Species:
9606
(Homo sapiens) [
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NKCDVVVVGGGISGMAAAKLLHDSGLNVVVLEARDRVGGRTYTLRNQKVK
YVDLGGSYVGPTQNRILRLAKELGLETYKVNEVERLIHHVKGKSYPFRGP
FPPVWNPITYLDHNNFWRTMDDMGREIPSDAPWKAPLAEEWDNMTMKELL
DKLCWTESAKQLATLFVNLCVTAETHEVSALWFLWYVKQCGGTTRIISTT
NGGQERKFVGGSGQVSERIMDLLGDRVKLERPVIYIDQTRENVLVETLNH
EMYEAKYVISAIPPTLGMKIHFNPPLPMMRNQMITRVPLGSVIKCIVYYK
EPFWRKKDYCGTMIIDGEEAPVAYTLDDTKPEGNYAAIMGFILAHKARKL
ARLTKEERLKKLCELYAKVLGSLEALEPVHYEEKNWCEEQYSGGCYTTYF
PPGILTQYGRVLRQPVDRIYFAGTETATHWSGYMEGAVEAGERAAREILH
AMGKIPEDEIWQSEPESVDVPAQPITTTFLERHLPSVPGLLRLIGLTTI
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
1s3e Chain A Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1s3e
Crystal Structures of Monoamine Oxidase B in Complex with Four Inhibitors of the N-Propargylaminoindan Class.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
V10 G11 G13 S15 L33 E34 A35 R36 G41 R42 G57 G58 S59 Y60 P234 V235 I264 W388 Y393 C397 Y398 G425 T426 G434 Y435 M436
Binding residue
(residue number reindexed from 1)
V8 G9 G11 S13 L31 E32 A33 R34 G39 R40 G55 G56 S57 Y58 P232 V233 I262 W386 Y391 C395 Y396 G423 T424 G432 Y433 M434
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G62 R197 K296
Catalytic site (residue number reindexed from 1)
G60 R195 K294
Enzyme Commision number
1.4.3.21
: primary-amine oxidase.
1.4.3.4
: monoamine oxidase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008131
primary methylamine oxidase activity
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0050660
flavin adenine dinucleotide binding
GO:0052595
aliphatic amine oxidase activity
GO:0097621
monoamine oxidase activity
Biological Process
GO:0009410
response to xenobiotic stimulus
GO:0009636
response to toxic substance
GO:0010044
response to aluminum ion
GO:0010269
response to selenium ion
GO:0014063
negative regulation of serotonin secretion
GO:0019607
phenylethylamine catabolic process
GO:0021762
substantia nigra development
GO:0032496
response to lipopolysaccharide
GO:0042420
dopamine catabolic process
GO:0045471
response to ethanol
GO:0045964
positive regulation of dopamine metabolic process
GO:0048545
response to steroid hormone
GO:0050665
hydrogen peroxide biosynthetic process
GO:0051412
response to corticosterone
Cellular Component
GO:0005739
mitochondrion
GO:0005740
mitochondrial envelope
GO:0005741
mitochondrial outer membrane
GO:0030425
dendrite
GO:0043025
neuronal cell body
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1s3e
,
PDBe:1s3e
,
PDBj:1s3e
PDBsum
1s3e
PubMed
15027868
UniProt
P27338
|AOFB_HUMAN Amine oxidase [flavin-containing] B (Gene Name=MAOB)
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